13127-82-7

Basic information

• Product Name: POE (2) OLEYL AMINE
• Synonyms: 2,2’-(9-octadecenylimino)bis-,(Z)-Ethanol;2’-(9-octadecenylimino)bis-(z)-ethano;N,N-bis(2-Hydroxyethyl)oleylamine;(Z)-2,2'-(octadec-9-enylimino)bisethanol;Ethanol, 2,2-(9Z)-9-octadecenyliminobis-;2,2'-[(Z)-9-Octadecenylimino]bisethanol;2,2'-[[(Z)-9-Octadecenyl]imino]bisethanol;Oleyl Amine Ethoxylate Ether (15EO)
• CAS NO: 13127-82-7
• Molecular Formula: C₂₂H₄₅NO₂
• Molecular Weight: 355.5982
• EINECS: 236-062-2
• Mol File: 13127-82-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 480.5 °C at 760 mmHg
• Flash Point: 202.6 °C
• Appearance: /
• Density: 0.917 g/cm³
• PKA: 14.41±0.10(Predicted)
• CAS DataBase Reference: POE (2) OLEYL AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: POE (2) OLEYL AMINE(13127-82-7)
• EPA Substance Registry System: POE (2) OLEYL AMINE(13127-82-7)

Safety Data

• Hazardous Substances Data: 13127-82-7(Hazardous Substances Data)

Usage

Uses

2,2''-(Oleylamino)diethanol can be used for antimicrobial applications.

Synthetic route

cis-1-chloro-9-octadecene (59485-81-3, 16507-61-2) + 2,2'-iminobis[ethanol] (111-42-2) → N,N-bis(2-hydroxyethyl)oleylamine (13127-82-7)

Conditions	Yield
With Tetrahydrofurfuryl alcohol

oleoyl alcohol (143-28-2) → N,N-bis(2-hydroxyethyl)oleylamine (13127-82-7)

Conditions	Yield
Multi-step reaction with 2 steps 1: thionyl chloride 2: tetrahydrofurfuryl alcohol View Scheme

N,N-bis(2-hydroxyethyl)oleylamine (13127-82-7) + salicylic acid (69-72-7) + molybdenum(VI) oxide → 2C22H43NO2(2-)*2C7H5O3(1-)*Mo(6+)

Conditions	Yield
In water at 95℃; for 1h; Inert atmosphere;

Upstream product

• 143-28-2 oleoyl alcohol 
• 59485-81-3 cis-1-chloro-9-octadecene 
• 111-42-2 2,2'-iminobis[ethanol] 

Relevant articles and documents

COMPOUNDS, COMPOSITONS AND METHODS RELATED TO ANTIMICROBIAL APPLICATIONS

The present disclosure is in the field of polymers and pharmaceuticals/antimicrobials. The disclosure provides compounds based on SNAP (synthetic novel antimicrobial polymer) technology, compositions and methods of managing microbial infections including surgical site infections (SSIs). The present compounds are used as a management/therapeutic strategy to target microbial infections and have advantages including excellent antimicrobial potency, biofilm disruption ability, broad spectrum activity against various organisms covering both gram negative and gram positive bacteria as well as fungal pathogens, and low toxicity profile to ensure a healthy therapeutic window for use in humans.

Phosphorous amine lubricant additives

Lubricant additives are produced by reacting an alkoxylated amine with phosphorous acid. The additives preferably also contain a boron moiety which is reacted with the phosphorous acid and amine, preferably in a one step reaction. More preferably, a mono-functional alcohol or a long-chain aliphatic carboxylic acid is added to this mixture. The additives are particularly useful in metal working oils and particularly as extreme pressure additives to replace the currently used chlorinated paraffin additives.